Canonical Allele Identifier:
CA1968513070
Gene:
Linked Data
dbSNP Id:
rs1856778742
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.45506612T>G , CM000673.2:g.45506612T>G | GRCh38 |
| NC_000011.9:g.45528162T>G , CM000673.1:g.45528162T>G | GRCh37 |
| NC_000011.8:g.45484738T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001748204.2:n.909-16841A>C | ||
| XR_931245.3:n.566-16841A>C |